Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss-Reference-Cited by-同舟云学术

Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss

Published:2019-04-23 Issue:6 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Li Xinlei¹^ORCID,Tan Bo¹,Wang Xiaoqian²,Xu Xiaofei¹,Wang Cuicui¹,Zhong Mingjun¹,Zhao Qiuling¹,Bao Zhongwei¹,Peng Weihua¹,Zhang Lei¹,Cheng Jing¹,Lu Yu¹,Wu Peina²,Yuan Huijun¹^ORCID

Affiliation:

1. Medical Genetics Center Southwest Hospital, Army Medical University Chongqing China

2. Department of Otorhinolaryngology Head and Neck Surgery Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences Guangzhou China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.685

Reference16 articles.

1. Genomic Landscape and Mutational Signatures of Deafness-Associated Genes

2. Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3;Bonne‐Tamir B.;The American Journal of Human Genetics,1996

3. Identification of a Novel Homozygous Mutation, TMPRSS3: c.535G>A, in a Tibetan Family with Autosomal Recessive Non-Syndromic Hearing Loss

4. Identification ofTMPRSS3as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

5. Newborn Hearing Screening — A Silent Revolution

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1. Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History;Audiology and Neurotology;2023

2. TMPRSS3 Gene Variants With Implications for Auditory Treatment and Counseling;Frontiers in Genetics;2021-11-19